Canonical Allele Identifier: CA2749314499
Gene: PCARE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.29070996_29070997insACA , CM000664.2:g.29070996_29070997insACA GRCh38
NC_000002.11:g.29293862_29293863insACA , CM000664.1:g.29293862_29293863insACA GRCh37
NC_000002.10:g.29147366_29147367insACA NCBI36
NG_021427.1:g.8265_8266insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000331664.6:c.3265_3266insTGT MANE Select ENSP00000332809.4:p.Pro1089delinsLeuSer
ENST00000331664.5:c.3265_3266insTGT ENSP00000332809.4:p.Pro1089delinsLeuSer
NM_001029883.2:c.3265_3266insTGT NP_001025054.1:p.Pro1089delinsLeuSer
XM_011532826.1:c.3265_3266insTGT XP_011531128.1:p.Pro1089delinsLeuSer
XR_939901.1:n.185+1829_185+1830insACA
XR_939902.1:n.173+1841_173+1842insACA
NM_001029883.3:c.3265_3266insTGT MANE Select NP_001025054.1:p.Pro1089delinsLeuSer
Search 100 bp 5'
Search 100 bp 3'